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Hydrochloric Acid → 2-Benzyloxy-5-(2-hydroxyethyl)benzamide

HRID 1862621
ノート
印刷プレビュー

反応式

HRID 1862621 の反応式
[CH2:1]([O:8][C:9]1[CH:17]=[CH:16][C:15]([CH2:18][CH2:19][O:20]COC)=[CH:14][C:10]=1[C:11]([NH2:13])=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.O>CO>[CH2:1]([O:8][C:9]1[CH:17]=[CH:16][C:15]([CH2:18][CH2:19][OH:20])=[CH:14][C:10]=1[C:11]([NH2:13])=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 962WaterHCID 186201822-Benzyloxy-5-(2-methoxymethoxyethyl)benzamide

生成物 1

HCID 186200672-Benzyloxy-5-(2-hydroxyethyl)benzamide収率 83.7%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of 2-benzyloxy-5-(2-methoxymethoxyethyl)benzamide (721 mg) in methanol (10 ml) was added concentrated hydrochloric acid (0.7 ml), and the mixture was heated under reflux for 1 hour with stirring. Water was added to the reaction mixture, and the resulting mixture was extracted with ethyl acetate. The extract was washed with brine and dried over anhydrous magnesium sulfate. After the solvent was removed under reduced pressure, diethyl ether was added to the residue, and the resulting insoluble material was collected by filtration to give 2-benzyloxy-5-(2-hydroxyethyl)benzamide (519 mg).

後処理

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 1 hour
  3. extractionthe resulting mixture was extracted with ethyl acetate
  4. washThe extract was washed with brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customAfter the solvent was removed under reduced pressure, diethyl ether
  7. additionwas added to the residue
  8. filtrationthe resulting insoluble material was collected by filtration

出典と根拠

ORDレコード
ord-2ae88990561d415f98aaa082d9a66f12
出典データセット
uspto-grants-2003_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06538152B1

反応ノート

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